TY - JOUR T1 - ON THE MECHANISM OF INTESTINAL ABSORPTION OF DRUGS JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 275 LP - 282 VL - 125 IS - 4 AU - C. Adrian M. Hogben AU - Dominick J. Tocco AU - Bernard B. Brodie AU - Lewis S. Schanker Y1 - 1959/04/01 UR - http://jpet.aspetjournals.org/content/125/4/275.abstract N2 - The intestinal absorption of acidic drugs is decreased severalfold and the absorption of basic drugs increased severalfold when the pH of the intestinal contents is raised from 4 to 8. This supports the hypothesis that the intestinal mucosa preferentially allows the absorption of the unionized form of a drug. Significant steady state concentration gradients of drugs are maintained between the gut lumen and plasma. Bases are concentrated within the gut lumen and acids are concentrated in plasma. These concentration ratios can be attributed to a slightly acidic environment at the intestinalblood barrier. There is a sufficient association between absorption of drugs and the lipid: water partition coefficients of their unionized moieties to justify the continued assumption that the gastrointestinal cell membranes are essentially lipoidal. Highly lipid-soluble drugs are in general rapidly absorbed while decidedly lipid-insoluble drugs are in general poorly absorbed. ER -